HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrochloric Acid → 2-(5-t-Butylfuran-2-yl)-cyclopropanecarboxylic acid
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Sodium Chloride | HCID 5234 | — |
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | Ethyl 2-(5-t-butylfuran-2-yl)-cyclopropanecarboxylate | HCID 20139954 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Water | HCID 962 | — |
| Product | 2-(5-t-Butylfuran-2-yl)-cyclopropanecarboxylic acid | HCID 20139962 | 100.6% |
Reaction Steps
Ethyl 2-(5-t-butylfuran-2-yl)-cyclopropanecarboxylate (5.0 g, 0.021 mol) was dissolved in methanol (50 ml) and a solution of potassium hydroxide (2.4 g, 0.043 mol) in water (50 ml) was added dropwise at room temperature. The solution was refluxed for 3 hours, cooled to room temperature and carefully neutralised with 2M HCl. Saturated sodium chloride was added, the aqueous solution extracted with ethyl acetate (4×50 ml) and dried over anhydrous sodium sulphate. Removal of the solvent gave 2-(5-t-butylfuran-2-yl)-cyclopropanecarboxylic acid (4.4 g, 100%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04743602 |
| Source dataset | uspto-grants-1988_05 |
| ORD ID | ord-4ff0c7d047714c218b904091b047059d |
| Source note | uspto-grants-1988_05 |